Product Wiki · Recalls · Health Canada — Medical Devices

Powerheart AED G5 — recall 77474

Health Canada — Medical Devices · Canada · 2025-05-21 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
77474
Date of alert
2025-05-21
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Cardiovascular
Product type
Medical devices
Reported risk: Notify users of the potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity). Ensure that users monitor the device's self-test status to mitigate clinical failures. Recall start date: February 27, 2025
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/powerheart-aed-g5

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